ComplianceOnline

Medical Devices: Reimbursement Strategies for North America and Abroad

Instructor: Mike Colvin
Product ID: 705635
  • Duration: 90 Min
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Customer Care

Fax: +1-650-362-2367

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This medical device reimbursement webinar will discuss the similarities and differences in reimbursements between US and abroad. It will teach how to develop the domestic and international strategies for effective reimbursement.

Why Should You Attend:

In general, all commercial medical devices require regulatory approval, for obvious reasons. Of equal importance, is to have a reimbursement pathway in each country where the device sale is targeted. Understanding the reimbursement strategies is critical for short and long-term success of the industry.

The objective of the Webinar is to teach participants how to develop their domestic and international strategies for effective reimbursement in parallel to achieving Regulatory Approval. Reimbursement can be just as important to obtaining Regulatory approval for the success of a company.

Areas Covered in the Webinar:

  • Similarities and differences in reimbursement between the US and abroad
  • DRG’s, HRG’s, CPT’s, HTA’s, and centralized vs. non-centralized reimbursement
  • How does one change the reimbursement posture?
  • Introducing new medical procedures and or technologies
  • How to effectively manage future reimbursement?

Who Will Benefit:

Anyone with a desire to be up to date with the current state of the art of domestic and international reimbursement for medical devices and combination products. Tiltes include:

  • Medical Industry Managers and Supervisors
  • Quality Assurance Personnel
  • Marketing Personnel
  • Strategic Planners
  • Technical Consultants
  • Regulatory Personnel
Instructor Profile:
Mike Colvin

Mike Colvin
Medical Device Technical Adviser/Consultant

Dr. Mike Colvin has over 30 years direct experience in managing Biocompatibility assessment and testing, working in the medical device and combination products field. He has worked on/contributed to many domestic and international Biocompatibility committees, and has been a consultant to the medical device industry on the proper Biocompatibility strategies for success.

Follow us :
IEC 60601-1 (3.1) The New Paradigm
Vendor and Supplier Qualification Program for FDA Regulated Industries

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

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